Relationships between acute hepatic porphyrias due to genetic variability of primary enzyme defects and limiting function of uroporphyrinogen synthase
- 31 December 1978
- journal article
- research article
- Published by Elsevier in International Journal of Biochemistry
- Vol. 9 (12), 911-916
- https://doi.org/10.1016/0020-711x(78)90069-1
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- Reduced Ferrochelatase Activity: a Defect Common to Porphyria Variegata and ProtoporphyriaBritish Journal of Haematology, 1977
- THE PRIMARY ENZYME DEFECT IN HEREDITARY COPROPORPHYRIAThe Lancet, 1976